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The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood

Negative symptoms predict adverse outcomes within psychotic disorders, in individuals at high-risk for psychosis, and in young people in the community. There is considerable interest in the dimensional structure of negative symptoms in clinical samples, and accumulating evidence suggests a 5-factor...

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Autores principales: Havers, Laura, Cardno, Alastair, Freeman, Daniel, Ronald, Angelica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827402/
https://www.ncbi.nlm.nih.gov/pubmed/35156042
http://dx.doi.org/10.1093/schizbullopen/sgac009
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author Havers, Laura
Cardno, Alastair
Freeman, Daniel
Ronald, Angelica
author_facet Havers, Laura
Cardno, Alastair
Freeman, Daniel
Ronald, Angelica
author_sort Havers, Laura
collection PubMed
description Negative symptoms predict adverse outcomes within psychotic disorders, in individuals at high-risk for psychosis, and in young people in the community. There is considerable interest in the dimensional structure of negative symptoms in clinical samples, and accumulating evidence suggests a 5-factor structure. Little is known about the underlying structure of negative symptoms in young people despite the importance of this developmental stage for mental health. We used confirmatory factor analysis to test the structure of parent-reported negative symptoms at mean ages 16.32 (SD 0.68, N = 4974), 17.06 (SD 0.88, N = 1469) and 22.30 (SD 0.93, N = 5179) in a community sample. Given previously reported associations between total negative symptoms and genome-wide polygenic scores (GPS) for major depressive disorder (MDD) and schizophrenia in adolescence, we assessed associations between individual subdomains and these GPSs. A 5-factor model of flat affect, alogia, avolition, anhedonia, and asociality provided the best fit at each age and was invariant over time. The results of our linear regression analyses showed associations between MDD GPS with avolition, flat affect, anhedonia, and asociality, and between schizophrenia GPS with avolition and flat affect. We showed that a 5-factor structure of negative symptoms is present from ages 16 to 22 in the community. Avolition was most consistently associated with polygenic liability to MDD and schizophrenia, and alogia was least associated. These findings highlight the value of dissecting negative symptoms into psychometrically derived subdomains and may offer insights into early manifestation of genetic risk for MDD and schizophrenia.
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spelling pubmed-88274022022-02-10 The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood Havers, Laura Cardno, Alastair Freeman, Daniel Ronald, Angelica Schizophr Bull Open Regular Article Negative symptoms predict adverse outcomes within psychotic disorders, in individuals at high-risk for psychosis, and in young people in the community. There is considerable interest in the dimensional structure of negative symptoms in clinical samples, and accumulating evidence suggests a 5-factor structure. Little is known about the underlying structure of negative symptoms in young people despite the importance of this developmental stage for mental health. We used confirmatory factor analysis to test the structure of parent-reported negative symptoms at mean ages 16.32 (SD 0.68, N = 4974), 17.06 (SD 0.88, N = 1469) and 22.30 (SD 0.93, N = 5179) in a community sample. Given previously reported associations between total negative symptoms and genome-wide polygenic scores (GPS) for major depressive disorder (MDD) and schizophrenia in adolescence, we assessed associations between individual subdomains and these GPSs. A 5-factor model of flat affect, alogia, avolition, anhedonia, and asociality provided the best fit at each age and was invariant over time. The results of our linear regression analyses showed associations between MDD GPS with avolition, flat affect, anhedonia, and asociality, and between schizophrenia GPS with avolition and flat affect. We showed that a 5-factor structure of negative symptoms is present from ages 16 to 22 in the community. Avolition was most consistently associated with polygenic liability to MDD and schizophrenia, and alogia was least associated. These findings highlight the value of dissecting negative symptoms into psychometrically derived subdomains and may offer insights into early manifestation of genetic risk for MDD and schizophrenia. Oxford University Press 2022-01-12 /pmc/articles/PMC8827402/ /pubmed/35156042 http://dx.doi.org/10.1093/schizbullopen/sgac009 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the University of Maryland's school of medicine, Maryland Psychiatric Research Center. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Article
Havers, Laura
Cardno, Alastair
Freeman, Daniel
Ronald, Angelica
The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood
title The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood
title_full The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood
title_fullStr The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood
title_full_unstemmed The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood
title_short The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood
title_sort latent structure of negative symptoms in the general population in adolescence and emerging adulthood
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827402/
https://www.ncbi.nlm.nih.gov/pubmed/35156042
http://dx.doi.org/10.1093/schizbullopen/sgac009
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